Devices and methods for facilitating sleeve gastrectomy procedures

ABSTRACT

A gastrectomy device includes an elongated member and a tube. The elongated member has a proximal end and a distal end and defines a longitudinal side window disposed adjacent the distal end. The elongated member defines a first longitudinal channel, a second longitudinal channel, and a plurality of side apertures. The first longitudinal channel is in communication with the longitudinal side window and the plurality of side apertures is in communication with the second longitudinal channel. The tube extends through the first longitudinal channel. An array of lights is associated with the tube to provide illumination. The tube is movable through the elongated member between a first state, in which the tube is disposed within the first longitudinal channel of the elongated member, and a second state, in which a portion of the tube extends through the longitudinal side window of the elongated member.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 14/521,571 filed Oct. 23, 2014, which claims the benefit of U.S. Provisional Patent Application Ser. No. 62/059,298, filed Oct. 3, 2014, the entire contents of each of which is incorporated by reference herein.

This application is a Continuation-In-Part of U.S. patent application Ser. No. 14/492,712, filed on Sep. 22, 2014, now U.S. Pat. No. 9,655,758, which claims the benefit of U.S. Provisional Patent Application Ser. No. 61/902,463, filed Nov. 11, 2013, the entire contents of each of which is incorporated by reference herein.

This application is also a Continuation-In-Part of U.S. patent application Ser. No. 14/491,660, filed on Sep. 19, 2014, which claims the benefit of U.S. Provisional Patent Application Ser. No. 61/901,870, filed Nov. 8, 2013, the entire contents of each of which is incorporated by reference herein.

TECHNICAL FIELD

The present disclosure relates generally to bariatric surgery and, more particularly, to devices and methods that facilitate performing sleeve gastrectomy procedures.

BACKGROUND

Obesity is reaching epidemic proportions in many regions of the world, particularly in the United States. In order to treat obesity, various surgical procedures have been developed including, for example, gastric bypass, adjustable gastric banding, and sleeve gastrectomy. The goal in each of these procedures is to reduce the patient's stomach capacity to restrict the amount of food that the patient can eat. The reduced stomach capacity, in turn, results in a feeling of fullness for the patient after ingesting a relatively smaller amount of food. Thus, the patient can achieve significant weight loss.

Sleeve gastrectomy involves transecting the stomach, e.g., using a stapling device or other suitable device, to reduce the patient's stomach volume. Sleeve gastrectomy procedures are often aided by the use of a bougie, which serves as a guide or template for transecting the stomach to the appropriate configuration while inhibiting inadvertent transection of stomach or esophageal tissue. Once the stomach has been appropriately transected, the bougie is removed and a leak test is performed to determine whether there are any areas of extravasation.

SUMMARY

Gastrectomy devices for use in bariatric surgery are provided in accordance with the present disclosure.

In embodiments, a gastrectomy device includes an elongated flexible tube member, a balloon member, and a shape modification member.

In embodiments, a gastrectomy device includes a shaft having at least one expandable feature.

In some embodiments, a gastrectomy device includes at least one stapling location identifying feature.

In another aspect of the present disclosure, another embodiment of a gastrectomy device is provided. The gastrectomy device includes an elongated member, a tube, and an array of lights. The elongated member has a proximal end and a distal end. The elongated member defines a longitudinal side window disposed adjacent the distal end, a first longitudinal channel in communication with the longitudinal side window, a plurality of side apertures, and a second longitudinal channel in communication with the plurality of side apertures. The second longitudinal channel is configured for coupling to a source of pressure. The tube extends through the first longitudinal channel and has a proximal end and a distal end. The array of lights is associated with the tube to provide illumination. The tube is movable through the elongated member between a first state, in which the tube is disposed within the first longitudinal channel of the elongated member, and a second state, in which a portion of the tube extends through the longitudinal side window of the elongated member.

In some embodiments, the gastrectomy device may further include an elongated printed circuit board disposed within the tube. The printed circuit board has the array of lights disposed thereon. It is contemplated that the array of lights may be LEDs.

It is envisioned that the gastrectomy device may further include a handle assembly coupled to the proximal end of the elongated member. The tube may be translatable through the handle assembly. The handle assembly may include a power source. In some embodiments, the power source may be a battery. The battery may be electrically connected to the array of lights. The handle assembly may include an activation strip removably coupled to the handle assembly.

In some embodiments, the handle assembly may include a luer assembly in fluid communication with the second longitudinal channel of the elongated member. The luer assembly may be configured for connection to the source of pressure. In some embodiments, the source of pressure may provide positive or negative pressure. In embodiments, the source of pressure may be a vacuum source or an insufflation source.

It is contemplated that the distal end of the elongated member may have a wireless receiver.

In some embodiments, the elongated member may be formed of a flexible material.

It is envisioned that the elongated member may form an arc in the second state.

In some aspects of the present disclosure, the tube may have an actuator fixed to the proximal end thereof.

In another aspect of the present disclosure, a method of performing bariatric surgery is provided. The method includes inserting the gastrectomy device into an oral cavity of a patient, guiding the gastrectomy device along an enteral pathway, repositioning the gastrectomy device based on an observed position of the illuminated tube to a selected position within a stomach of the patient, moving the tube from a first state to a second state, in which the tube bows outwardly through the longitudinal side window of the elongated member into engagement with a portion of the stomach, and transecting a portion of the stomach.

In some embodiments, guiding the gastrectomy device along the enteral pathway may include advancing the gastrectomy device from an oral cavity through an esophagus into an antrum of the stomach.

It is contemplated that the method may further include at least one of: insufflating fluid through the second longitudinal channel and out of the plurality of side apertures; or vacuuming fluid from the antrum of the stomach through the plurality of side apertures and into the second longitudinal channel.

In some embodiments, moving the tube may include sliding the proximal end of the tube distally relative to the elongated member through the first longitudinal channel.

BRIEF DESCRIPTION OF THE DRAWINGS

Various aspects and features of the present disclosure are described herein with reference to the drawings wherein:

FIGS. 1-11 are progressive views of various embodiments of gastrectomy devices for effectuating gastrectomy procedures involving shape modification and/or remodeling;

FIGS. 12-31 are views illustrating various embodiments of gastrectomy devices with a shafts having expandable features;

FIGS. 32-41 are views illustrating various embodiments of gastrectomy devices including stapling location identifying features;

FIG. 42 shows a pair of perspective views of one embodiment of a gastrectomy device, one of the pair of perspective views showing the gastrectomy device in a first state, the other of the pair of perspective views showing the gastrectomy device in a second state;

FIG. 43 shows a distal end portion of the gastrectomy device of FIG. 42 in the second state in a patient's stomach;

FIGS. 44 and 45 show perspective views of various embodiments of gastrectomy devices in first and second states;

FIG. 46 is a perspective view, with parts separated, of another embodiment of a gastrectomy device in accordance with the principles of the present disclosure;

FIG. 47 is a cutaway view of a handle assembly of the gastrectomy device of FIG. 46;

FIG. 48 is a perspective view of the gastrectomy device of FIG. 46 illustrating a tube thereof in a first, unexpanded state; and

FIG. 49 is an enlarged view of the gastrectomy device of FIG. 46 illustrating the tube in a second, expanded state.

DETAILED DESCRIPTION OF EMBODIMENTS

Embodiments of the present disclosure are detailed below with reference to the drawings in which like reference numerals designate identical or corresponding elements in each of the several views. Throughout this description, the term “proximal” will refer to the portion of the device or component thereof that is closest to the user and the term “distal” will refer to the portion of the device or component thereof that is farthest from the user.

As depicted in FIGS. 1-11, embodiments of sleeve gastrectomy devices are provided in accordance with the present disclosure for effectuating gastrectomy procedures involving shape modification and/or remodeling.

Turning now to FIG. 1, one embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 10. Device 10 includes a tubular member 12 and an expandable balloon 14 supported on a distal end of tubular member 12. Tubular member 12 defines an aperture 12 a through which a magnetic member 16 of device 10 can be advanced. Balloon 14 is selectively inflatable and deflatable, for example, in the antrum of the stomach “S” to position device 10 for effectuating a sleeve gastrectomy procedure. Magnetic member 16 includes a distal end portion 16 a that supports one or more magnets 18 and/or magnetic material and a proximal end portion 16 b. Magnetic member is advanced out of device 10 so that distal end portion 16 a is positioned against an internal surface of stomach “S” for remodeling a curvature of stomach “S.” A manipulation tool 20 having a shaft 22 that supports a capturing portion 24 can be positioned on an external surface of stomach “S” adjacent to distal end portion 16 a of magnetic member 16 to magnetically secure distal end portion 16 a to stomach “S.” The stomach “S” can then be resected, as appropriate, separating the stomach “S” into a resected portion “R” and a new stomach portion “SN.” One skilled in the art will realize that any number of open or laparoscopic stomach resection techniques/devices can be used including surgical staplers, vessel sealing devices, suturing and scalpels, etc. At some point prior to removal of device 10 and/or manipulation tool 20, the new stomach portion “SN” is tested for extravasation using any suitable technique, for example, by insufflating with saline and/or a dye, etc. The resected portion “R” can then be removed with distal end portion 16 a, which is severed at proximal end portion 16 b during resection, upon withdrawing manipulation tool 20 and balloon 14 can be deflated so that device 10 can be withdrawn.

As seen in FIG. 2, another embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 30. Device 30 includes a tubular member 32 and an expandable balloon 34 supported on a distal end of tubular member 32. Tubular member 32 defines a first aperture 32 a and a second aperture 32 b. A form wire 36 is supported on tubular member 32 by suture 38. Form wire 36 includes a first wire anchor 36 a on a distal end thereof and a second wire anchor 36 b on a proximal end thereof. Suture 38 includes a first portion 38 a and a second portion 38 b, each of which may be separate sutures. To support form wire 36 on tubular member 32, first portion 38 a extends through first aperture 32 a and is secured to a distal end portion of form wire 36 and second portion 38 b extends through second aperture 32 b and is secured to a proximal end portion form wire 36.

Similar to balloon 14, balloon 34 is selectively inflated in the antrum of stomach “S” to position device 30 for effectuating a sleeve gastrectomy procedure. Suture 38 is advanced out of device 30 so that form wire 36 separates from tubular member 32 and spring biases against an internal surface of stomach “S” so that wire anchors 36 a and 36 b secure form wire 36 to stomach “S” for remodeling a curvature of stomach “S.” The stomach “S” can then be resected, as appropriate, separating the stomach “S” into a resected portion “R” and a new stomach portion “SN.” The new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” can be grasped by a separate forceps “F” and removed with form wire 36, which is separated from tubular member 32 when the suture 38 is severed during resection, and balloon 34 can be deflated so that device 30 can be withdrawn.

Turning now to FIG. 3, yet another embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 40. Device 40 includes a tubular member 42 and an expandable balloon 44 supported on a distal end of tubular member 42. Tubular member 42 defines an aperture 42 a. A rigid forming member 46 is advanceable through tubular member 42 and out of aperture 42 a and has a suture 48 secured to a proximal end portion thereof. Rigid forming member 46 includes a first anchor 46 a on a distal end thereof and a second anchor 46 b on a proximal end thereof.

Similar to balloon 14, balloon 44 is selectively inflated in the antrum of stomach “S” to position device 40 for effectuating a sleeve gastrectomy procedure. Rigid forming member 46 is advanced out of device 40 until suture 48 extends through aperture 42 a so that first anchor 46 a of rigid forming member 46 can be positioned against an internal surface of stomach “S.” A separate forceps “F” can then grasp rigid forming member 46 from an external surface of stomach “S” to support rigid forming member 46 against stomach “S.” Then, rigid forming member 46 can be positioned flush against the internal surface of stomach “S” so that anchors 46 a, 46 b and forceps “F,” which is positioned centrally on rigid forming member 46, secure rigid forming member 46 to stomach “S” for remodeling a curvature of stomach “S.” Stomach “S” can then be resected, as appropriate, separating the stomach “S” into a resected portion “R” and a new stomach portion “SN.” The new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” and rigid forming member 46, which is separated from tubular member 42 when suture 48 is severed during resection, can be removed by forceps “F,” and balloon 44 can be deflated so that device 40 can be withdrawn.

As seen in FIG. 4, one embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 50. Device 50 includes a tubular member 52 and a first expandable balloon 54 supported on a distal end of tubular member 52 and a second expandable balloon 56 supported on tubular member 52 proximally of first expandable balloon 54. The second balloon 56 can have a non-compliant shape. A distal end portion of second balloon 56 can be temporarily secured to tubular member 52 via suture 58.

Similar to balloon 14, balloon 54 is selectively inflated in the antrum of stomach “S” to position device 50 for effectuating a sleeve gastrectomy procedure. Second balloon 56 is inflated against an internal surface of stomach “S” for remodeling a curvature of stomach “S.” The stomach “S” can then be at least partially resected, as appropriate, separating the stomach “S” into a resected portion “R” and a new stomach portion “SN.” Before completion of the resection, first and second balloons 54, 56 can be deflated and device 50 can be withdrawn so that resection can be completed. Upon completion of the resection, the new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” can be grasped by a separate forceps “F” and removed.

Turning now to FIG. 5, still another embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 60. Device 60 includes a tubular member 62 and an expandable balloon 64 supported on a distal end of tubular member 62. Tubular member 62 defines an aperture 62 a, out of which, an articulating member 66 can be advanced. Articulating member 66 includes a distal end portion 66 a, a pivot portion 66 b, a proximal end portion 66 c, and an articulation pull wire 66 d that is secured to distal end portion 66 a.

Similar to balloon 14, balloon 64 is selectively inflated in the antrum of stomach “S” to position device 60 for effectuating a sleeve gastrectomy procedure. Distal end portion 66 a is advanced out of device 60 so that a proximally pulling of pull wire 66 d pivots distal end portion 66 a relative to proximal end portion 66 c about pivot portion 66 b to position distal end portion 66 a against an internal surface of stomach “S” for remodeling a curvature of stomach “S.” The stomach “S” can then be at least partially resected, as appropriate, separating the stomach “S” into a resected portion “R” and a new stomach portion “SN.” Before completion of the resection, articulation member 66 can be withdrawn so that resection can be completed. Upon completion of the resection, the new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” can be grasped by a separate forceps “F” and removed, and balloon 64 can be deflated so that device 60 can be withdrawn.

Turning now to FIG. 6, still another embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 70. Device 70 includes a tubular member 72 and an expandable balloon 74 supported on a distal end of tubular member 72. Tubular member 72 defines an aperture 72 a, out of which, an articulating spine 76 can be advanced. Articulating spine 76 includes a distal end portion 76 a and a plurality of vertebral members 76 b. Each vertebral member of the plurality of vertebral members 76 b defines a pull wire lumen 76 c dimensioned to receive a pull wire 76 d therethrough. The pull wire 76 d is secured to distal end portion 76 a, extends through each pull wire lumen 76 c, and couples the plurality of vertebral members 76 b together with distal end portion 76 a.

Similar to balloon 14, balloon 74 is selectively inflated in the antrum of stomach “S” to position device 70 for effectuating a sleeve gastrectomy procedure. Distal end portion 76 a and at least some of the plurality of vertebral members 76 b are advanced out of device 70 so that a proximal pulling of pull wire 76 d articulates articulating spine 76 to that at least some of the plurality of vertebral members 76 b abut against an internal surface of stomach “S” for remodeling a curvature of stomach “S,” which can be a predetermined curvature. The stomach “S” can then be at least partially resected, as appropriate, separating the stomach “S” into a resected portion “R” and a new stomach portion “SN.” Before completion of the resection, articulation spine 76 can be withdrawn so that resection can be completed. Upon completion of the resection, the new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” can be grasped by a separate forceps and removed, and balloon 74 can be deflated so that device 70 can be withdrawn.

As seen in FIG. 7, yet another embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 80. Device 80 includes a tubular member 82 and an expandable balloon 84 supported on a distal end of tubular member 82. Tubular member 82 defines an aperture 82 a, out of which, a flexible wire form 86 can be advanced.

Similar to balloon 14, balloon 84 is selectively inflated in the antrum of stomach “S” to position device 80 for effectuating a sleeve gastrectomy procedure. Flexible wire form 86 is advanced out of device 80 and into an internal surface of stomach “S.” The flexibility of flexible wire form 86 enables flexible wire form 86 to curve into any suitable shape for remodeling a curvature of stomach “S.” For example, flexible wire form 86 can be advanced against stomach “S” and curled to form a B-shape with a first looped portion 86 a and a second looped portion 86 b that cooperate to remodel the curvature of stomach “S” for resection. Stomach “S” can then be at least partially resected, as appropriate, separating the stomach “S” into a resected portion “R” and a new stomach portion “SN.” Before completion of the resection, flexible wire form 86 can be withdrawn so that resection can be completed. Upon completion of the resection, the new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” can be grasped by a separate forceps and removed, and balloon 84 can be deflated so that device 80 can be withdrawn.

Turning now to FIG. 8, device 80 can include a rigid wire form 88 instead of flexible wire form 86. Rigid wire form 88 includes a curved distal end portion 88 a that is advanced out of device 80 and against stomach “S” to remodel a curvature of stomach “S.” Similar to that described above, stomach “S” can then be at least partially resected, as appropriate, separating the stomach “S” into a resected portion “R” and a new stomach portion “SN.” Before completion of the resection, rigid wire form 88 can be withdrawn so that resection can be completed. Upon completion of the resection, the new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” can be grasped by a separate forceps and removed, and balloon 84 can be deflated so that device 80 can be withdrawn.

As seen in FIG. 9, one embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 90. Device 90 includes a tubular member 92 and an expandable balloon 94 supported on a distal end of tubular member 92. Tubular member 92 includes a distal end portion 92 a and a proximal end portion 92 b supported on distal end portion 92 a. Proximal end portion 92 b is positioned around distal end portion 92 a to define a passage 92 c therebetween that is dimensioned to receive a wire-forming loop 96.

Similar to balloon 14, balloon 94 is selectively inflated in the antrum of stomach “S” to position device 90 for effectuating a sleeve gastrectomy procedure. Wire forming loop 96 is advanced out of passage 92 c and into an internal surface of stomach “S.” Wire forming loop 96 defines a loop 96 a that increases in diameter as wire-forming loop 96 is distally advanced from passage 92 c and into contact with an internal surface of stomach “S” for remodeling the curvature of stomach “S” for resection. Stomach “S” can then be resected, as appropriate, while retracting wire-forming loop 96 to decrease the diameter of loop 96 a as resection (e.g., stapling and cutting) progresses. The decrease in diameter of loop 96 a may be indexed, for example, to correlate with the staple line formed in the stomach “S” during resection. The resection separates the stomach “S” into a resected portion “R” and a new stomach portion “SN.” Before completion of the resection, Wire forming loop 96 can be withdrawn so that resection can be completed. Upon completion of the resection, the new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” can be grasped by a separate forceps and removed, and balloon 94 can be deflated so that device 90 can be withdrawn.

Turning now to FIG. 10, another embodiment of a sleeve gastrectomy device is shown generally identified by reference numeral 100. Device 100 includes a tubular member 102 and an expandable balloon 104 supported on a distal end of tubular member 102. Tubular member 102 defines an attachment point 102 a and supports a loop collar 106 dimensioned to linearly translate about an outer surface of tubular member 102. Loop collar 106 includes a collar 106 a, wire member 106 b, and an actuation rod 106 c. Wire member 106 b extends along an outer surface of tubular member 102 and is secured to attachment point 102 a at a proximal end of wire member 106 b and to collar 106 a at a distal end of wire member 106 b. A distal end of actuation rod 106 c is secured to collar 106 a to move collar 106 linearly relative to tubular member 102 upon linear translation of actuation rod 106 c. Actuation rod 106 c extends along tubular member 102 and can be arranged to extend along the outer surface of tubular member 102 and/or through tubular member 102. Tubular member 102 can define a channel (not shown) therealong to facilitate linear movement of collar 106 a.

Similar to balloon 14, balloon 104 is selectively inflated in the antrum of stomach “S” to position device 100 for effectuating a sleeve gastrectomy procedure. Actuation rod 106 c is pulled proximally to draw collar 106 a proximally. As collar 106 a moves proximally relative to tubular member 102, wire member 106 b extends outwardly forming a loop 108 that engages an internal surface of stomach “S” to remodel the curvature of stomach “S” for resection. Similar to that described above, stomach “S” can then be at least partially resected, as appropriate. As stapling and cutting progresses for the resection, actuation rod 106 c can be distally advanced to distally advance collar 106 a and tighten slack formed in wire member 106 b as loop 108 decreases in diameter. Ultimately, collar 106 a is advanced to a distal most position, e.g., the insertion position, so that wire 106 b is flush or substantially flush against tubular member 102 so that loop 108 can be retracted for final stapling and cutting. Upon completion of the resection, the stomach “S” is resected into a resected portion “R” and a new stomach portion “SN” that can be tested for extravasation as described above. The resected portion “R” can be grasped by a separate forceps and removed, and balloon 104 can be deflated so that device 100 can be withdrawn.

As seen in FIG. 11, an embodiment of a sleeve gastrectomy system is shown generally identified by reference numeral 110. System 110 includes a device 120 and grasping instrument 130. Device 120 includes a tubular member 122 and an expandable balloon 124 supported on a distal end of tubular member 122. Grasping instrument 130 includes an elongate body 132 and an end effector 134

Similar to balloon 14, balloon 124 is selectively inflated in the antrum of stomach “S” to position device 120 for effectuating a sleeve gastrectomy procedure. End effector 134 of grasping instrument 130 can be used to grasp a portion of stomach “S” to be removed upon resection. Similar to that described above, stomach “S” can then be resected into a resected portion “R” and a new stomach portion “SN.” Upon completion of the resection, the new stomach portion “SN” can be tested for extravasation as described above. The resected portion “R” can be removed by grasping instrument 130, and balloon 104 can be deflated so that device 120 can be withdrawn.

Turning now to FIGS. 12-31, embodiments of tubular members of sleeve gastrectomy devices can include at least one expandable feature to facilitate securement of the respective embodiments of gastrectomy devices within the stomach, for example, within the antrum of the stomach.

As shown in FIG. 12, one embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 140. Tubular member 140 includes an outer member 140 a and an inner member 140 b that defines a centerline “C.” Outer member 140 a includes a plurality of umbrella members 142 that are selectively expandable relative to centerline “C” between a contracted state and an expanded state in response to linear movement of outer member 140 a relative to inner member 140 b, as indicated by arrow “a.” Each umbrella member 142 can have the same and/or different outer diameters in the contracted and/or expanded states and each umbrella member 142 includes a plurality of segments 142 a that are positioned radially around tubular member 140. Each segment 142 a of the plurality of segments 142 a is spaced apart from the other segments 142 a of the plurality of segments when umbrella member 142 is disposed in the expanded state and can be in contact with adjacent segments 142 a when umbrella member 142 is in the contracted state. Tubular member 140 can be secured to vacuum source “VS” adapted to enable suction through one or more of the plurality of umbrella members 142 when in the expanded state.

As depicted in FIG. 13, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 150. Tubular member 150 includes a shaft 152 and a polymer braid 154 with a plurality of braided filaments 154 a secured to shaft 152. Shaft 152 defines a centerline “C.” Braid 154 is selectively expandable relative to centerline “C” between a contracted state and an expanded state in response to linear movement of braid 154 relative to shaft 152, as indicated by arrow “a.” Tubular member 150 can be secured to vacuum source “VS” adapted to enable suction between adjacent braided filaments 154 a of braid 154 when braid 154 is in the expanded state.

Turning now to FIG. 14, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 160. Tubular member 160 includes a shaft 162 that defines a centerline “C,” a compliant balloon 164 supported on shaft 162, and a plurality of vacuum tubes 166 supported on balloon 164 and extending along shaft 162. Compliant balloon 164 can be coupled to an inflation source “IS” that is adapted to deliver inflation fluid, e.g., saline, to balloon 164 for selectively expanding and/or contracting balloon 164 between a contracted state and an expanded state relative to centerline “C.” The plurality of vacuum tubes 166 defines a plurality of vacuum ports 166 a. A vacuum source “VS” can be coupled to vacuum tubes 166 to provide suction through vacuum ports 166 a.

As depicted in FIG. 15, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 170. Tubular member 170 includes a shaft 172 and a compliant balloon 174 supported on a side surface of shaft 172. Shaft 172 defines a centerline “C,” a plurality of vacuum ports 172 a, and vacuum lumen 172 b that extends along centerline “C” and is in fluid communication with the plurality of vacuum ports 172 a. A vacuum source “VS” can be coupled to vacuum lumen 172 b to provide suction through vacuum ports 172 a. Compliant balloon 174 is coupled to an inflation conduit 176 that extends along shaft 172 and can be coupled to an inflation source “IS” adapted to deliver inflation fluid, e.g., saline, to balloon 174 for selectively expanding and/or contracting balloon 174 between a contracted state and an expanded state relative to the side surface of shaft 172.

As seen in FIG. 16, yet another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 180. Tubular member 180 includes a shaft 182 and a plurality of compliant balloons 184 supported in spaced-apart relation radially around an outer surface of shaft 182. Shaft 182 defines a centerline “C” and a plurality of vacuum ports 186 positioned between adjacent balloons 184 of the plurality of compliant balloons 184. The plurality of vacuum ports 186 includes a first port 186 a, a second port 186 b, and a third port 186 c. Vacuum ports 186 are in fluid communication with a vacuum lumen 186 d defined by shaft 182. Vacuum lumen 186 d extends along centerline “C” of shaft 182. A vacuum source “VS” can be coupled to vacuum lumen 186 d to provide suction through the plurality of vacuum ports 186. The plurality of compliant balloons 184 includes a first balloon 184 a, a second balloon 184 b, and a third balloon 184 c. Each of the plurality of compliant balloons 184 is coupled to an inflation conduit 188 that extends along shaft 182 and can be coupled to an inflation source “IS” adapted to deliver inflation fluid, e.g., saline, to the balloons 184 for selectively expanding and/or contracting balloons 184 between a contracted state and an expanded state relative to the outer surface of shaft 182. A separate inflation conduit 188 can be coupled to each of first, second, and third balloons 184 a, 184 b, 184 c.

Turning now to FIG. 17, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 190. Tubular member 190 includes a shaft 192 and an expandable coil 194 helically supported around an outer surface of shaft 192. A distal end of expandable coil 194 is secured to a distal end portion of shaft 192 Shaft 192 defines a centerline “C,” and a plurality of vacuum ports 192 a, and vacuum lumen 192 b that extends along centerline “C” and is in fluid communication with the plurality of vacuum ports 192 a. A vacuum source “VS” can be coupled to vacuum lumen 192 b to provide suction through vacuum ports 192 a. As indicated by arrow “a,” expandable coil 194 can be linearly advanced along shaft 192 relative to centerline “C” for selectively expanding and/or contracting coil 194 between a contracted state, where coil 194 is adjacent to shaft 192, and an expanded state, where coil 194 is spaced from shaft 192. Adjacent turns of expandable coil 194 are closer to one another in the expanded state than in the contracted state, and vice versa.

As depicted in FIG. 18, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 200. Tubular member 200 includes an outer shaft 202 a, an inner shaft 202 b, and a rolling member 204 secured to a side surface of inner shaft 202 b along an edge of rolling member 204. Inner shaft 202 b defines a centerline “C” and a plurality of vacuum ports 206. In response to rotational movement of inner shaft 202 b, for example, in the direction indicated by arrow “b₁,” rolling member 204 is movable between a contracted state, where rolling member 204 is wrapped around inner shaft 202 b in an overlapping arrangement in close proximity to the centerline “C,” and an expanded state, where rolling member 204 is unraveled, for example in the direction indicated by arrow “b₂,” so that portions of rolling member 204 are farther from centerline “C” than those respective portions are in the contracted state. A vacuum source “VS” can be coupled to vacuum ports 206, for example, via a vacuum lumen (not shown) to provide suction through vacuum ports 206.

As seen in FIG. 19, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 210. Similar to tubular member 200, tubular member 210 can include a plurality of spaced apart rolling members such as rolling members 204 a-204 d, etc.

As depicted in FIG. 20, still another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 220. Tubular member 220 includes a shaft 222 and a plurality of spaced-apart balloons 224 that are selectively expandable relative to a centerline “C” defined by shaft 222 between contracted and expanded states. The plurality of balloons 224 can includes a first balloon 224 a, a second balloon 224 b, and a third balloon 224 c, etc., each of which can be coupled to one or more inflation conduits (not shown) defined by shaft 222 that are in fluid communication with an inflation source “IS.” Similar to that described above, shaft 222 defines a plurality of vacuum ports 222 a in fluid communication with a vacuum source “VS,” for example, via a vacuum lumen (not shown) defined by shaft 222 that couples to vacuum source “VS.”

Turning now to FIG. 21, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 230. Tubular member 230 includes a shaft 232 that supports a self-expanding member 234 and a linearly translatable sheath 236 supported on self-expanding member 234. Sheath 236 is retractable in the direction indicated by arrow “a” to free self-expanding member 234 to enable self-expanding member 234 to expand from a contracted state, where sheath 236 covers self-expanding member 234, to an expanded state, where sheath 236 is retracted. Self-expanding member 234 can be formed of a shape memory material such as nitinol and/or an electroactive polymer.

As seen in FIG. 22, still another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 240. Tubular member 240 includes a shaft 242 that defines a centerline “C” and supports an actuating assembly 244 and a blade assembly 246. Actuating assembly includes drive shaft 244 a that supports an actuator face 244 b on a distal end of drive shaft 244 a. Actuator face 244 b defines a plurality of channels 244 c and a plurality of passages 244 d. Blade assembly 246 includes a plurality of blades 246 a and defines vacuum ports 246 c between each blade 246 a of the plurality of blades 246 a. Each blade 246 a of the plurality of blades 246 a includes a finger 246 b extending proximally from a proximal end portion of blade 246 a. Each finger 246 b is received within one of the plurality of channels 244 c so that rotational movement of actuation assembly 244, for example, in the direction indicated by arrow “b,” rotates actuator face 244 b so that fingers 246 b of each blade 246 a slide through channels 244 c to rotate blade assembly 246 between expanded and contracted states relative to centerline “C.” Vacuum ports 246 c are in fluid communication with passages 244 d, which can be coupled to a vacuum source “VS,” as described above.

As seen in FIG. 23, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 250. Tubular member 250 includes an outer shaft 252, an inner shaft 254 supported within outer shaft 252, and a clover member 256 supported on outer shaft 252. Inner shaft 254 defines a centerline “C.” Clover member 256 includes a plurality of radially spaced-apart clovers 256 a and defines a central lumen 256 b. Inner shaft 254 is linearly translatable relative to outer shaft 252, as indicated by arrow “a,” into central lumen 256 b of clover member 256 so that the plurality of clovers 256 a expands radially outwardly relative to the centerline “C” from a contracted state to an expanded state. Clover member 256 defines a plurality of vacuum ports 258 between the plurality of clovers 256 a. Similar to that described above, vacuum ports 258 are in fluid communication with a vacuum source “VS” coupled to tubular member 250 at a proximal end portion thereof.

Turning now to FIG. 24, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 260. Tubular member 260 includes an inner shaft 262 that defines a centerline “C” and supports a plurality of stacked outer shafts 264 that are linearly translatable along centerline “C,” as indicated by arrow “a” in a telescoping arrangement. The plurality of stacked outer shafts 264 can include a first outer shaft 264 a, a second outer shaft 264 b, and a third outer shaft 264 c, etc., where each outer shaft has a different outer diameter with each successive outer diameter increasing in size so that tubular member 260 can expand from a contracted state, which can be defined by the diameter of the outer surface of inner shaft 262, to an expanded state, which can be defined the diameter of the outer surface of one of the plurality of stacked outer shafts 264. Any of the inner and/or outer shafts 262, 264 can define a plurality of vacuum ports 266 that can be disposed in fluid communication with a vacuum source “VS” as described above.

As seen in FIG. 25, one embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 270. Tubular member 270 includes a shaft 272 that defines a centerline “C,” a balloon member 274 supported on shaft 272 in fluid communication with an inflation source “IS,” and a foam member 276 supported on balloon member 274 that expands from a contracted state to an expanded state in response to inflation of balloon member 274 via inflation source “IS.” Foam member 276 is in fluid communication with one or more vacuum conduits 278 that are coupled to a vacuum source “VS” similar to that described above.

With reference to FIG. 26, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 280. Tubular member 280 includes an outer shaft 282 that defines a central lumen 282 a and a centerline “C” and includes a low durometer distal portion 282 b. Tubular member 280 supports a plurality of rods 284 that can be linearly advanced along centerline “C,” as indicated by arrow “a,” into a distal end portion of central lumen 282 a to expand distal portion 282 b of outer shaft 282 from a contracted state to an expanded state. Outer shaft 282 can define a plurality of vacuum ports 286 that are in fluid communication with a vacuum source “VS” as described above.

Turning now to FIG. 27, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 290. Tubular member 290 includes a shaft 292 that defines a centerline “C,” a plurality of expandable members 294, a plurality of rigid collars 296 interleaved between the plurality of expandable members 294, and an actuation rod 298 secured to a distal tip 292 a of shaft 292. Actuation rod 298 is linearly translatable relative to centerline “C,” as indicated by arrow “a” to compress expandable members 294 against rigid collars 296 thereby expanding expandable members 294 from a contracted state to an expanded state. Collars 296 can define vacuum ports 296 a that are in fluid communication with a vacuum source “VS,” similar to that described above.

As seen in FIG. 28, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 300. Tubular member 300 includes a shaft 302 that defines a centerline “C” and vacuum lumen 302 a in fluid communication with a vacuum source “VS” as described above. Shaft 302 supports a plurality of inner shafts 304, each of the plurality of inner shafts 304 includes a curved portion 304 a. Each inner shaft 304 of the plurality of inner shafts 304 is rotatable, as indicated by arrows “b,” so that curved portions 304 a rotate between a contracted state, where curved portions 304 a are inwardly directed, to an expanded state, where curved portions 304 a are outwardly directed.

With reference to FIG. 29, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 310. Tubular member 310 includes an outer shaft 312 a that defines a centerline “C” and an inner shaft 312 b that supports a clamshell assembly 314. One or both of inner and outer shafts 312 a, 312 b can define one or move vacuum ports (not shown) that are in fluid communication with a vacuum source “VS” similar to that described above. Clam shell assembly 314 includes a first shell 314 a and second shell 314 b that are pivotally coupled to an actuation rod 316 at pivot 314 c so that a rotational movement of actuation rod 316, as indicated by arrow “b,” moves clam shell assembly 314 between a contracted state, where first and second shells 314 a, 314 b are in close approximation with centerline “C,” and an expanded state, where first and second shells 314 a, 314 b are spaced from centerline “C.”

Turning now to FIG. 30, another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 320. Tubular member 320 includes a shaft 322 that defines a centerline “C,” a plurality of laser cut tubes 324 disposed on shaft 322, and a sheath 326 secured to the plurality of laser cut tubes 324 that is linearly movable relative to the plurality of laser cut tubes 324, as indicated by arrow “a.” Sheath 326 can define a plurality of vacuum ports 328 that are in fluid communication with a vacuum source “VS” similar to that described above. Each tube of the plurality of laser cut tubes 324 includes a plurality of tines 324 a disposed radially about the tube 324. Each tine of the plurality of tines 324 a is secured to sheath 326 so that linear movement of sheath 326 moves tines 324 a between a contracted state, where tines 324 a and sheath 326 are in close proximity to centerline “C” and an expanded state, where tines 324 a and sheath 326 are radially spaced from centerline “C.”

As seen in FIG. 31, still another embodiment of a distal end portion of a tubular member is shown generally identified by reference numeral 330. Tubular member 330 includes a shaft 332 has an expandable portion 332 a and defines a centerline “C,” a central lumen 332 b, and a plurality of vacuum ports 332 c. Shaft 332 supports a mandrel 334 that is linearly movable through central lumen 332 b, as indicated by arrow “a,” to move expandable portion 332 a between a contracted state and an expanded state, as indicated by arrows “b.” Mandrel 334 defines a plurality of flutes 334 a that extend along a length of mandrel 334 to provide a fluid communication between vacuum ports 332 c and a vacuum source “VS” coupled to a proximal end portion of tubular member 330, as described above.

FIGS. 32-41 are views illustrating various embodiments of gastrectomy devices including stapling location identifying features.

With reference to FIG. 32, device 120, described above, is shown with balloon 124 thereof inflated to fill antrum of stomach “S” to give a visual start indicator “I” for identifying a stapling location, which is shown, for example, at 6 centimeters. As can be appreciated, balloon 124 can be filled with any suitable biocompatible filler including, for example, air, saline, and/or foam.

As seen in FIG. 33, embodiments of gastrectomy devices, such as device 340, can include a shaft 340 a defining a channel 340 b and supporting a pivoting foot 340 c on a distal end portion of shaft 340 a. Device 340 is adapted to receive a rigid rod 342 that can be advanced through channel 340 to engage and pivot pivoting foot 340 c about pivot 340 d, as indicated by arrow “a.” Alternatively, or additionally, a suture 344 can be received in channel 340 that is secured to a proximal end of pivoting foot 340 c to pivot pivoting foot 340 c about pivot 340 d by pulling suture 344, as indicated by arrow “b.” In these embodiments, pivoting foot 340 c can be positioned in stomach “S” to give a visual start indicator “I,” as described above.

With reference to FIG. 34, embodiments of gastrectomy devices, such as device 350, can include a shaft 352 defining an aperture 352 a and supporting a wire form probe 354 that can be advanced out of aperture 352 a so that a dimple 354 a disposed on an end of probe 354 can engage an internal surface of stomach “S” to establish a visual start indicator “I,” as described above.

Turning now to FIG. 35, embodiments of gastrectomy devices, such as device 360, can include a shaft 362 defining an channel 362 a and supporting a tape probe 364 that can be advanced out of channel 362 a so that probe 364 can engage an internal surface of stomach “S” to establish a visual start indicator “I,” as described above.

As seen in FIGS. 36 and 37, embodiments of gastrectomy devices, such as device 370 and device 380 can include similar features. For example, device 370 includes a distal positioning basket 372 and device 380 includes a distal positioning pigtail 382, each of which can serve to establish a visual start indicator “I,” as described above.

With reference to FIG. 38, embodiments of gastrectomy devices can be utilized with additional instruments such as a laser device 390 that is adapted to provide a projected staple line with the laser “L.”

As depicted in FIG. 39, embodiments of gastrectomy devices can be utilized with additional instruments such as external position clamp 400. Clamp 400 can include a pivotable clamp 410 that is adapted to position an embodiment of a gastrectomy device in desired position in stomach “S” such as the antrum.

Turning now to FIGS. 40 and 41, embodiments of gastrectomy devices, such as device 420 and device 430 can also include features to help establish a visual start indicator. For example, device 420 includes an indicator device 422 such as an RF tag and/or a magnet that can communicate with a stapler relay “SR” to help identify a start position. Similarly, device 430 includes an LED indicator 432.

With reference to FIG. 42, another embodiment of a gastrectomy device is shown generally identified by reference numeral 440 which is a device for the purpose of predictably remodeling the anatomy of the stomach, particularly the greater curvature, such that the approximated anterior and posterior sides of the stomach are uniform during partial sleeve gastrectomy with repeatable results from case to case. Device 440 features a proximal handle assembly 442 connected to a flexible polymer main shaft 443 with a second more rigid polymer deflection shaft 444 positioned parallel to and tangent to polymer shaft 443. The length of the deflection shaft 444 is such that it connects proximally to the actuating member 446 of the handle assembly 442 and distally to the atraumatic polymer tip 445; both the main shaft 443 and deflection shaft 444 being attached to the atraumatic tip 445 fully distal. The design of both the main shaft 443 and deflection shaft 444 are each tubes of specific outer diameters and wall thicknesses, respectively. In order to achieve ease of actuation and a specific curvature of the deflection shaft 444, relief features may be included of depth and pattern to affect the necessary deployed geometry.

A plurality of coupling brackets 447 exist along the length of the main shaft 443 in order to maintain the position of the main shaft 443 to the deflection shaft 444 over the length of the device. The connection of the coupling brackets 447 are such that they are mounted securely to the main shaft 443 while allowing the deflection shaft 444 to move freely, linearly. The location of a coupling bracket 447 a dictates the resultant shape of the deflection shaft arc, and therefore can be spaced and positioned in a location(s) to maximize the effectiveness of the bow. A plurality of through lumens 448 in the main shaft exists at a specific distance from the distal end of the device over a specific length, and is oriented radial and perpendicular to the major axis of the shaft. The proximal handle assembly 442 includes a rigid, static handle 449 a and a rigid, dynamic actuating member 449 b. This actuating member 449 b is attached to the static handle 449 a in such a way as to be able to translate linearly over a specific distance. The deflection shaft 444 being attached to the actuation member 449 b, when translating from proximal to distal, advances through the coupling brackets 447 distally. The result is that as the deflection shaft 444 is loaded in compression, being constrained by the static length of the main shaft 443, and bows into an arc 444 a at the distal end of the device.

Within the handle assembly is a pressure regulator 441 that is linked to the inner lumen of the main shaft 443 through a lumen in the handle 442. A luer assembly 450 is also attached to the pressure regulator 441 in the handle 442 such that air can be introduced through the inner lumen of the main shaft 443 and through the lumens at the distal end 448 to achieve insufflation, or air withdrawn through this same path to achieve suction, both flow rates being controlled by the regulator 441. A length of LED lights 452 is housed within the ID of the deflection shaft 444 at the distal end of the device existing between the atraumatic tip 445 and the distal most coupling bracket 447 a.

Referring to FIG. 43, in use, the main shaft 443 of the device is introduced into the patient through the mouth, down the esophagus, cannulating the esophageal sphincter, and placed distally at the area of the antrum and pylorus. The user then orients the device rotationally via the proximal handle such that the main shaft 443 is oriented against the inner curve of the stomach “S” and the deflection shaft 444 is oriented toward the greater curve of the stomach. The actuation member on the handle assembly is then advanced distally, activating the LED light array and resulting in the bowing effect of the deflection shaft to the degree that the arc 444 a of the shaft interfaces with the greater curve, putting the anterior and posterior sides of the stomach in tension and uniform about the distal geometry of the device. The LED array creates a visual indicator to the surgeon of the placement of the bowed deflection shaft. Additionally, this deflection results in a resultant force causing the atraumatic distal end of the main shaft 443 to conform to the angularis and antrum. Suction is then applied through the main shaft 443, pulling the inner surfaces of the lesser curve against the perforated distal length of the main shaft 443 and deflating the stomach “S.” This vacuum results in making the remodeled stomach static, to which the handle actuation member can be returned to its fully proximal position, retracting the bow of the deflection member and returning it tangent to the main shaft 443. As the main shaft 443 exists from the antrum, along the lesser curve, to the cardia, it serves as a visual template to the surgeon performing the resection procedure laparoscopically. This, along with the LED array, is a visual guide for application of the staple line over the resected stomach. Once the resection is completed, the device allows for pressure testing of the newly remodeled sleeve by ceasing suction and allowing for insufflation of the sleeve cavity to a specific pressure. Upon completion of the procedure, the device is removed from the patient. This LED array feature can be included as an element in any of the embodiments.

With reference to FIG. 44, one embodiment of a gastrectomy device is shown generally identified by reference numeral 460 which similar to device 440 but includes a compliant balloon feature 462 is located at the distal end of the device and can be inflated via a lumen that runs from the handle, through the ID of the main shaft 443 to the balloon.

In use, the main shaft 443 of the device is introduced into the patient through the mouth, down the esophagus, cannulating the esophageal sphincter, and placed distally at the area of the antrum and pylorus. The user then orients the device rotationally via the proximal handle such that the main shaft 443 is oriented against the inner curve of the stomach and the deflection shaft is oriented toward the greater curve of the stomach. The actuation member 449 b on the handle assembly 442 is then advanced distally, resulting in the bowing effect of the deflection shaft to the degree that the arc 444 a of the shaft interfaces with the greater curve, putting the anterior and posterior sides of the stomach in tension and uniform about the distal geometry of the device. Additionally, this deflection results in a resultant force causing the atraumatic distal end of the main shaft 443 to conform to the angularis and antrum. The distal balloon 462 is then inflated to a specific volume that results in the balloon filling the antrum and positioning the distal end of the device a specific distance from the pylorus. This is the starting point to begin resection. Suction is then applied through the main shaft 443, pulling the inner surfaces of the lesser curve against the perforated distal length of the main shaft 443 and deflating the stomach. This vacuum results in making the remodeled stomach static, to which the handle actuation member 449 b can be returned to its fully proximal position, retracting the arc 444 a of the deflection member 444 and returning it tangent to the main shaft 443. As the main shaft 443 exists from the antrum, along the lesser curve, to the cardia, it serves as a visual template to the surgeon performing the resection procedure laparoscopically. Once the resection is completed and the balloon 462 deflated, the device allows for pressure testing of the newly remodeled sleeve by ceasing suction and allowing for insufflation of the sleeve cavity to a specific pressure. Upon completion of the procedure, the device is removed from the patient.

Turning now to FIG. 45, one embodiment of a gastrectomy device is shown generally identified by reference numeral 470 which similar to devices 440 and 460 but includes a pivot stress relief feature 471 located at a specific distance from the distal end of the main shaft 443 and an actuation wire 472 that travels to and through a lumen in the handle attached to the atraumatic tip 445 and within the ID of the main shaft 443.

In use, the main shaft 443 of the device is introduced into the patient through the mouth, down the esophagus, cannulating the esophageal sphincter, and placed distally at the area of the antrum and pylorus. The user then orients the device rotationally via the proximal handle such that the main shaft 443 is oriented against the inner curve of the stomach and the deflection shaft 444 is oriented toward the greater curve of the stomach. The actuation member 449 b on the handle assembly 442 is then advanced distally, resulting in the bowing effect of the deflection shaft 444 to the degree that the arc of the shaft interfaces with the greater curve, putting the anterior and posterior sides of the stomach in tension and uniform about the distal geometry of the device. The actuation wire 472 is put in tension by the user, which deflects the distal end of the main shaft 443, pivoting about the pivot feature 471 and seating the distal end of the device in the antrum. Additionally, this deflection results in a resultant force causing the atraumatic distal end of the main shaft 443 to conform to the angularis and antrum. Suction is then applied through the main shaft 443, pulling the inner surfaces of the lesser curve against the perforated distal length of the main shaft 443 and deflating the stomach. This vacuum results in making the remodeled stomach static, to which the handle actuation member 449 b can be returned to its fully proximal position, retracting the arc 444 a of the deflection member 444 and returning it tangent to the main shaft 443. As tension is still applied to the actuation wire 472, the deflection of the main shaft 443 remains seated at the antrum and serves as an indicator to start resection. This is a visual guide for application of the staple line over the resected stomach. Once the resection is completed, the device allows for pressure testing of the newly remodeled sleeve by ceasing suction and allowing for insufflation of the sleeve cavity to a specific pressure. Upon completion of the procedure, tension of the actuation wire 472 is released and the device is removed from the patient.

FIGS. 46-49 illustrate another embodiment of a gastrectomy device shown generally as reference numeral 500. Gastrectomy device 500 is similar to gastrectomy device 460. Gastrectomy device 500 generally includes a handle assembly 510, an elongated member 540 extending distally from handle assembly 510, and a tube 560 associated with elongated member 540. Handle assembly 510 has a first section 512 a and a second section 512 b coupled to first section 512 a and together defining a longitudinal passageway 514 that extends through handle assembly 510. A saddle member 516 attaches to first and second sections 512 a, 512 b. Saddle 516 has protruding, surface features 518 configured to enhance a clinician's ability to grip handle assembly 510 with one hand.

Handle assembly 510 includes a battery housing 520 and a battery, for example, a pair of batteries 522 a, 522 b configured for snap-fit engagement within battery housing 520. Batteries 522 a, 522 b are positioned within battery housing 520. An actuation strip 524 is fabricated from a non-conductive material and received in battery housing 520 through a slit 526 defined in saddle 516. Actuation strip 524 isolates batteries 522 a, 522 b from each other such that power is not transmitted therebetween. Prior to use of gastrectomy device 500, actuation strip 524 is removed from slit 526 to electrically connect batteries 522 a, 522 b. Once connected, batteries 522 a, 522 b provide power to lights 570 as discussed in detail below.

Handle assembly 510 includes a luer assembly 528 having a first end 530 a extending outside of handle assembly 510 and a second end 530 b disposed within longitudinal passageway 514 of handle assembly 510. First end 530 a is configured for connection to a pressure source. Pressure source includes one of a positive pressure source, such as, for example, an insufflation source “FS” (FIG. 48), or a negative pressure source, such as, for example, a vacuum source “VS” (FIG. 48). Second end 530 b is in communication with a second longitudinal channel 548 of elongated member 540. As such, fluid (e.g., air) can be directed into second longitudinal channel 548 of elongated member 540 or fluid may be directed out of elongated member 540. Luer assembly 528 has a pressure regulator 532 including a bellows 534 and a biasing member 536 disposed between luer assembly 528 and bellow 534. Pressure regulator 532 relieves pressure from within second longitudinal channel 548 upon the pressure reaching a threshold limit.

Elongated member 540 defines a longitudinal axis “X” and has a proximal end 542 a and a distal end 542 b. Elongated member 540 is fabricated from a flexible material, for example, a suitable elastomer, adapted to conform to an interior of a stomach. Proximal end 542 a is disposed within handle assembly 510 and distal end 542 b is disposed distally of handle assembly 510. Elongated member 540 defines a longitudinal side window 544, a first longitudinal channel 546, a second longitudinal channel 548, and a plurality of side apertures 550. Side window 544 is disposed adjacent distal end 542 b and has an opening large enough to accommodate passage of tube 560, as described in greater detail below. First longitudinal channel 546 is in communication with side window 544 and is configured for disposal of tube 560.

Second longitudinal channel 548 of elongated member 540 is fluidly isolated from first longitudinal channel 546 by a septum (not shown) and extends in parallel relation to first longitudinal channel 546. Second longitudinal channel 548 is in fluid communication with side apertures 550 and luer assembly 528. As such, upon connecting insufflation source “FS” to first end 530 a of luer assembly 528, fluid (i.e., air) may be directed from luer assembly 528 through second longitudinal channel 548, and out of side apertures 550. Additionally, upon connecting a vacuum source “VS” to first end 530 a of luer assembly 528, suction may be provided at side apertures 550.

Distal end 542 b of elongated member 540 has a cap 552 attached thereto. Cap 552 has a cylindrical extension 554 defining a cavity 556 configured for mating engagement with a distal end 562 b of tube 560. Cap 552 houses a GPS receiver 558. GPS receiver 558 enables a clinician to identify the precise location of a distal end of gastrectomy device 500 within a patient. In some embodiments, various wireless fiduciary markers may be supported by cap 552 to determine a location of cap 552 and thus gastrectomy device 500.

With continued reference to FIGS. 46-49, tube 560 is formed from a semi-rigid, resiliently flexible and transparent material, e.g., a suitable elastomer. Tube 560 defines a length greater than the length of elongated member 540 such that tube 560 can be accessed outside the patient and/or remotely of the surgical site. Tube 560 extends through handle assembly 510 and through first longitudinal channel 546 of elongated member 540. Tube 560 has a proximal end 562 a extending proximally from handle assembly 510 and a distal end 562 b. Proximal and distal ends 562 a, 562 b of tube 560 are interconnected to one another via a coupling member 563. In some embodiments proximal and distal ends 562 a, 562 b of tube 560 may be monolithically formed with one another. Proximal end 562 a of tube 560 has an actuator 564. Actuator 564 defines a pair of depressions 566 disposed on opposite sides of actuator 564 configured for manipulation by fingers of a clinician.

With reference to FIGS. 48 and 49, distal end 562 b of tube 560 is integrally, i.e., monolithically, formed with or otherwise fixedly mated to cap 552 of elongated member 540 such that distal movement of tube 560 causes distal end 562 b of tube 560 to expand or bow outwardly relative to elongated member 540. More specifically, distal movement of tube 560 causes a portion 566 of tube 560 to move from a first state, as shown in FIG. 48, in which tube 560 is disposed within first longitudinal channel 546 of elongated member 540 and parallel with longitudinal axis “X,” to a second state, as shown in FIG. 49, in which portion 566 of tube 560 extends outwardly from elongated member 540. In the second state, portion 566 of tube 560 extends through longitudinal side window 544 of elongated member 540 to form an arc. In the second state, tube 560 defines a configuration that generally complements the curvature of a greater curvature portion of a stomach. Translating tube 560 proximally relative to elongated member 540 pulls portion 566 of tube 560 into first longitudinal channel 546 through side window 544.

With reference to FIG. 46, gastrectomy device 500 further includes an array of lights 570 associated with tube 560. Lights 570 provide a visual reference of the position of tube 560 and/or gastrectomy device 500 generally. In some embodiments, lights 570 may be integrally formed with tube 560. An elongated printed circuit board 572 is disposed within tube 560 and has lights 570 supported thereon. Printed circuit board 572 may be configured to frictionally fit within tube 560 such that printed circuit board 572, with lights 570 disposed thereon, move with tube 560. Printed circuit board 572 is made of a pliable material that permits printed circuit board 572 to flex as tube 560 moves between the first, unexpanded state, to the second, expanded state. A cable 574 extends from printed circuit board 572 to electrically connect lights 570 to a power source. Power source may be in the form of batteries, such as, for example, AAA batteries 522 a, 522 b, or some other power source to supply power to lights 570. It is contemplated that lights 570 may include an integral power source or may be wirelessly coupled (i.e., inductively) to a source of power that is external to the patient. A sheath 576 surrounds and encloses distal end 562 b of tube 560 and lights 570.

In operation, with tube 560 in the first, unexpanded state, as shown in FIG. 48, gastrectomy device 100 is inserted into a patient, such as, for example, an oral cavity of a patient and is distally advanced toward a stomach of the patient along an enteral pathway that extends from the oral cavity, through an esophagus of the patient, and into the stomach. Lights 570 are powered by power source 522 a, 522 b to illuminate tube 560 and/or gastrectomy device 500 generally. With tube 560 illuminated, gastrectomy device 500 is guided along the enteral pathway via observation of the illuminated tube 560. Gastrectomy device 500 is selectively repositioned based on observed positions of the illuminated tube 560 along the enteral pathway. Guidance of gastrectomy device 500 through the esophagus is further aided by GPS receiver 558 supported in distal cap 552. Gastrectomy device 500 is further guided through the esophagus and selectively positioned within the stomach of the patient.

Upon positioning gastrectomy device 500 within the stomach, a clinician grips actuator 564 supported on proximal end 562 a of tube 560 and translates tube 560 distally, in the direction indicated by arrow “B” in FIG. 48, through handle assembly 510 and first longitudinal channel 546 of elongated member 540. Distal movement of tube 560, in conjunction with distal end 562 b of tube 560 being fixed relative to distal end 542 b of elongated member 540, causes tube 560 to bow outwardly relative to elongated member 540 and through side window 544 towards the expanded state, as shown in FIG. 49. As tube 560 bows outwardly towards the expanded state, elongated member 540 is urged towards and into complementary mating relation with a lesser curvature portion of the stomach, while tube 560 is urged towards and into complementary mating relation with a greater curvature portion of the stomach. As such, the orientation of gastrectomy device 500 with elongated member 540 extending along the lesser curvature portion of the stomach between the esophageal sphincter and the pyloric sphincter can be readily achieved. As a result of this configuration of gastrectomy device 500 in the expanded state, the above-described orientation of gastrectomy device 500 within the stomach is maintained despite spasms, folding, spiraling, and/or shifting of the stomach.

Once the proper orientation of elongated member 540 has been achieved, suction is applied, by a vacuum source “VS,” within second longitudinal channel 548 of elongated member 540 for suctioning any remaining contents within the antrum of the stomach into second longitudinal channel 548 of elongated member 540 through side apertures 550. Application of suction within second longitudinal channel 548 also suctions the lesser curvature portion of the stomach to an outer surface of elongated member 540, to ensure and maintain the complementary mating relation of elongated member 540 with the lesser curvature portion of the stomach.

With elongated member 540 maintained in position relative to the lesser curvature portion of the stomach as a result of the applied suction, proximal end 562 a of tube 560 is translated proximally relative to elongated member 540 such that tube 560 is pulled into first longitudinal channel 546 through side window 544 to return to the first, unexpanded state. As suction is maintained at this point, elongated member 540 is maintained in the position detailed above despite contraction of tube 560.

Once tube 560 has been returned to the unexpanded state (i.e., disposed coaxial with longitudinal axis “X”), transection of the stomach adjacent elongated member 540 on an opposite side of elongated member 540 relative to the lesser curvature portion of the stomach may be effected in any suitable fashion, e.g., using a stapling device or other suitable device. Transection in this manner reforms the stomach to a tubular-shaped configuration that generally approximates the outer dimension of elongated member 540 and extends between the esophageal sphincter and the pyloric sphincter. As can be appreciated, the diameter of elongated member 540 may be selected in accordance with a desired diameter of the tubular-shape reformed stomach.

Further aspects of the present disclosure can be appreciated from the following numbered paragraphs: 1. A gastric guide, comprising: an elongated member having a proximal end and a distal end, the elongated member a longitudinal channel in communication with a plurality of apertures; a flexible sail member having an array of lights extending along the sail member, the sail member being attached at a distal end to the distal end of the elongated member and having a proximal portion that is slidable with respect to the elongate member.

2. The gastric guide according to paragraph 1, further comprising a vacuum source coupled to the longitudinal channel.

3. The gastric guide according to paragraph 1, wherein the elongated member defines a window and a passageway, the sail member being disposed in the passageway.

4. The gastric guide according to paragraph 1, further comprising a GPS receiver.

5. The gastric guide according to paragraph 1, wherein the sail member is configured to bow outwardly when the proximal portion is moved proximally with respect to the elongated member, the sail automatically assuming the shape of the greater curvature of the stomach.

6. The gastric guide according to paragraph 6, wherein the sail member has a bulging region and a tapering region when the proximal portion is moved proximally with respect to the elongated member.

7. The gastric guide according to paragraph 1, wherein the sail member is a transparent tube.

8. The gastric guide according to paragraph 7, wherein the array of lights is disposed in the tube.

It will be understood that various modifications may be made to the embodiments of the present disclosure herein. Therefore, the above description should not be construed as limiting, but merely as exemplifications of embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the present disclosure. 

The invention claimed is:
 1. A gastrectomy device, comprising: an elongated member defining: a longitudinal side window disposed adjacent a distal end portion of the elongated member; a first longitudinal channel in communication with the longitudinal side window; a plurality of side apertures; and a second longitudinal channel in communication with the plurality of side apertures and configured for coupling to a source of pressure; a tube extending through the first longitudinal channel, wherein the tube is movable to bow outwardly through the longitudinal side window; and an array of lights associated with the tube to provide illumination.
 2. The gastrectomy device of claim 1, further including an elongated printed circuit board disposed within the tube and having the array of lights disposed thereon.
 3. The gastrectomy device of claim 1, wherein the array of lights includes LEDs.
 4. The gastrectomy device of claim 1, further including a handle assembly coupled to a proximal end portion of the elongated member, the tube being translatable through the handle assembly.
 5. The gastrectomy device according to claim 4, wherein the handle assembly includes a power source electrically connected to the array of lights.
 6. The gastrectomy device of claim 5, wherein the power source includes a battery.
 7. The gastrectomy device of claim 6, further including an activation strip removably coupled to the handle assembly.
 8. The gastrectomy device of claim 4, wherein the handle assembly includes a luer assembly in fluid communication with the second longitudinal channel of the elongated member, the luer assembly being configured for connection to the source of pressure.
 9. The gastrectomy device of claim 8, wherein the source of pressure provides at least one of negative pressure or positive pressure at the plurality of side apertures.
 10. The gastrectomy device of claim 1, wherein the distal end portion of the elongated member has a wireless receiver.
 11. The gastrectomy device of claim 1, wherein the tube is formed of a flexible material.
 12. The gastrectomy device of claim 1, further including an indicator device selected from the group consisting of an RF tag and a magnet. 